Search Results - Mohammad Ali Faghihi

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  1. 1
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    De-repressing LncRNA-Targeted Genes to Upregulate Gene Expression: Focus on Small Molecule Therapeutics by Roya Pedram Fatemi, Dmitry Velmeshev, Mohammad Ali Faghihi

    Published 2014
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  2. 2
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    Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran by Marzieh Nejabat, Soroor Inaloo, Afsaneh Taghipour Sheshdeh, Shima Bahramjahan, Fatima Masoomi Sarvestani, Pegah Katibeh, Hamid Nemati, Hamid Nemati, Seyed Mohammad Bagher Tabei, Mohammad Ali Faghihi, Mohammad Ali Faghihi

    Published 2021
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  3. 3
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    Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

    Published 2017
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  4. 4
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    A novel stop-gain mutation in DPYS gene causing Dihidropyrimidinase deficiency, a case report by Malihe Mirzaei, Arghavan Kavosi, Mahboobeh Sharifzadeh, Ghazale Mahjoub, Mohammad Ali Faghihi, Parham Habibzadeh, Majid Yavarian

    Published 2020
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  5. 5
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    Generalized exfoliative skin rash as an early predictor of supratherapeutic voriconazole trough levels in a leukemic child: A case report by Ali Amanati, Parisa Badiee, Mehrzad Lotfi, Ahmad Monabati, Mohammad Ali Faghihi, Majid Yavarian, Nazafarin Hatami-Mazinani

    Published 2020
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  6. 6
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    A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis by Mohammad Reza Bordbar, Farzaneh Modarresi, Mohammad Ali Farazi Fard, Hassan Dastsooz, Nader Shakib Azad, Mohammad Ali Faghihi

    Published 2017
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  7. 7
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    Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report by Fatemeh Maghami, Seyed Mohammad Bagher Tabei, Hossein Moravej, Hassan Dastsooz, Farzaneh Modarresi, Mohammad Silawi, Mohammad Ali Faghihi

    Published 2018
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  8. 8
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    An immunocompetent patient with a nonsense mutation in NHEJ1 gene by Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi

    Published 2019
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  9. 9
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    A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report by Soheila Zareifar, Hassan Dastsooz, Mahdi Shahriari, Mohammad Ali Faghihi, Golsa Shekarkhar, Mohammadreza Bordbar, Omid Reza Zekavat, Nader Shakibazad

    Published 2019
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  10. 10
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    Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene by Parvaneh Karimzadeh, Samaneh Naderi, Farzaneh Modarresi, Hassan Dastsooz, Hamid Nemati, Tayebeh Farokhashtiani, Bibi Shahin Shamsian, Soroor Inaloo, Mohammad Ali Faghihi

    Published 2017
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  11. 11
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    A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome by Maryam Taghdiri, Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei, Majid Fardaei, Majid Fardaei, Sanaz Mohammadi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi

    Published 2017
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  12. 12
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    Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series by Ghazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, Malihe Mirzaei, Arghavan Kavosi, Laila Jamali, Haniyeh Javanmardi, Pegah Katibeh, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Published 2019
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  13. 13
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    A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report by Fateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, Parham Habibzadeh, Hamid Nemati, Amir Saeed, Mohammad Silawi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Published 2019
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  14. 14
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    A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report by Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Hassan Dastsooz, Mohammad Silawi, Mohammad Ali Farazi Fard, Ali Adib, Ali Kafashan, Zahra Tabatabaei, Forough Sadeghipour, Mohammad Ali Faghihi

    Published 2018
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  15. 15
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    Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene by Parham Habibzadeh, Zahra Tabatabaei, Mohammad Ali Farazi Fard, Laila Jamali, Aazam Hafizi, Pooneh Nikuei, Leila Salarian, Mohammad Hossein Nasr Esfahani, Zahra Anvar, Mohammad Ali Faghihi

    Published 2020
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  16. 16
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    Molecular Function and Regulation of Non-coding RNAs in Multifactorial Diseases by Mohammadreza Hajjari

    Published 2016
    Other Authors: “…Mohammad Ali Faghihi…”
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